Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_provenance.
- NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_assertion description "[Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_provenance.
- NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_assertion evidence source_evidence_literature NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_provenance.
- NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_assertion SIO_000772 2562820 NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_provenance.
- NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_assertion wasDerivedFrom befree-20150227 NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_provenance.
- NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_assertion wasGeneratedBy ECO_0000203 NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP244400.RAeRvt0BAhmgK5oQUVwQnv3UMH7LxRmv1U5oHZ-t4L2q4130_provenance.